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rs730880590

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880590(A;A)
Make rs730880590(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position47333219
GeneMYBPC3
is asnp
is mentioned by
dbSNPrs730880590
ebirs730880590
HLIrs730880590
Exacrs730880590
Varsomers730880590
Maprs730880590
PheGenIrs730880590
hapmaprs730880590
1000 genomesrs730880590
hgdprs730880590
ensemblrs730880590
gopubmedrs730880590
geneviewrs730880590
scholarrs730880590
googlers730880590
pharmgkbrs730880590
gwascentralrs730880590
openSNPrs730880590
23andMers730880590
23andMe allrs730880590
SNP Nexus

SNPshotrs730880590
SNPdbers730880590
MSV3drs730880590
GWAS Ctlgrs730880590
Max Magnitude0
ClinVar
Risk rs730880590(A;A)
Alt rs730880590(A;A)
Reference rs730880590(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYBPC3
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.47354770A>T
CLNSRC
CLNACC RCV000158225.1,